Known targets — ChEMBL curated mechanism
ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Acetic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Similar compounds — the chemically nearest patent molecules
Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Acetic Acid SCHEMBL5819597 | 1.00 | FFAR3 (0.50) | — | |
| Acetic Acid SCHEMBL4574765 | 0.97 | FFAR3 (0.47) | — | |
| Acetic Acid SCHEMBL6335654 | 0.91 | FFAR3 (0.41) | — | |
| Hexane SCHEMBL2705931 | 0.88 | AKR1B1 (0.48) | — | |
| Acetic Acid SCHEMBL5358874 | 0.86 | FFAR3 (0.37) | — | |
| Acetic Acid SCHEMBL6509092 | 0.86 | FFAR3 (0.37) | — | |
| Oxalic Acid SCHEMBL17224590 | 0.86 | ALOX15 (0.42) | — | |
| Oxalic Acid SCHEMBL17224587 | 0.86 | ALOX15 (0.42) | — | |
| Methacrylic Acid SCHEMBL331477 | 0.82 | ALDH1A1 (0.38) | — | |
| SCHEMBL48849 | 0.80 | — | — |
Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.
Patent provenance — the patents this molecule appears in, and who filed them
Claimed or disclosed in 72 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114685471-A | Preparation method of isoxazoline compound | 沈阳科创化学品有限公司 | 2022-07-01 | — | — | CN | claimed |
| CN-105061304-A | Method for preparing isoxazoline compound and intermediate thereof | SHENYANG SCIENCREAT CHEMICALS CO LTD | 2015-11-18 | — | — | CN | claimed |
| US-20260109657-A1 | USE OF POLYAMINES IN THE PRETREATMENT OF BIOMASS | UNIV CALIFORNIA (US) | 2026-04-23 | — | — | US | disclosed |
| US-12492155-B2 | Use of polyamines in the pretreatment of biomass | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2025-12-09 | — | — | US | disclosed |
| US-20250369183-A1 | USE OF IN-SITU IONIC LIQUID (IL) AND DEEP EUTECTIC SOLVENT (DES) SYNTHESIS USING CHEMICALLY SYNTHESIZED OR BIOMASS-DERIVED IONS IN THE PRETREATMENT OF BIOMASS | UNIV CALIFORNIA (US) | 2025-12-04 | — | — | US | disclosed |
| US-20250353988-A1 | DEPOLYMERIZATION OF LIGNIN USING A SUPPORTED METAL CATALYST | U.S. DEPARTMENT OF ENERGY | 2025-11-20 | — | — | US | disclosed |
| US-20250326706-A1 | METHODS AND COMPOSITIONS USEFUL FOR OXIDATION OF BIOMASS TO CARBOXYLIC ACIDS USING POLYOXOMETALATE IONIC LIQUIDS | UNIV CALIFORNIA (US) | 2025-10-23 | — | — | US | disclosed |
| US-12392085-B2 | Use of in-situ ionic liquid (IL) and deep eutectic solvent (DES) synthesis using chemically synthesized or biomass-derived ions in the pretreatment of biomass | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2025-08-19 | — | — | US | disclosed |
| US-20250243523-A1 | USE OF METAL SALTS AND DEEP EUTECTIC SOLVENTS IN A PROCESS TO SOLUBILIZE A BIOMASS | U.S. DEPARTMENT OF ENERGY | 2025-07-31 | — | — | US | disclosed |
| EP-4590722-A1 | METHODS AND COMPOSITIONS USEFUL FOR FRACTIONATING BIOMASS USING A SCHIFF-BASE IONIC LIQUID | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2025-07-30 | — | — | EP | disclosed |
| US-12371855-B2 | Use of ensiled biomass for increased efficiency of the pretreatment of biomass | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2025-07-29 | — | — | US | disclosed |
| EP-0396378-A1 | Antifungal agent | MERCK & CO. INC. (US) | 1990-11-07 | — | — | EP | disclosed |
| US-4952604-A | GLYCINE ESTERS OF 2-(ISODEC-1,3,5-TRIENYL), 4-METHOXY,5-METHYL-TETRAHYDROPYRAN-3-OL | MERCK & CO., INC. (US) | 1990-08-28 | — | — | US | disclosed |
| US-4588734-A | ENZYME INHIBITORS | USV PHARMACEUTICAL CORP. (US) | 1986-05-13 | — | — | US | disclosed |
| US-4565825-A | Antihypertensive N-benzimidazolyl- and N-imidazolyl-amino acid derivatives | USV PHARMACEUTICAL CORP. (US) | 1986-01-21 | — | — | US | disclosed |
| US-4548928-A | ANGIOTENSIN INHIBITORS | USV PHARMACEUTICAL CO. (US) | 1985-10-22 | — | — | US | disclosed |
| US-4507312-A | Antihypertensive amides | USV PHARMACEUTICAL CORPORATION (US) | 1985-03-26 | — | — | US | disclosed |
| EP-0083186-A2 | Thiazole derivatives as H2-receptor antagonists | ELI LILLY AND COMPANY (US) | 1983-07-06 | — | — | EP | disclosed |
| US-4304771-A | N-SULFUR-CONTAINING HETEROCYCLE SUBSTITUTED | USV PHARMACEUTICAL CORPORATION (US) | 1981-12-08 | — | — | US | disclosed |
| US-4256761-A | Antihypertensive amides | USV PHARMACEUTICAL CORPORATION (US) | 1981-03-17 | — | — | US | disclosed |